4.4 Article

Expression of developmentally regulated plasma membrane polypeptide (DREPP2) in rice root tip and interaction with Ca2+/CaM complex and microtubule

Journal

PROTOPLASMA
Volume 252, Issue 6, Pages 1519-1527

Publisher

SPRINGER WIEN
DOI: 10.1007/s00709-015-0781-x

Keywords

Ca2+-binding protein; Calmodulin; Cell elongation; DREPP; Microtubule; Oryza sativa; Salt stress

Funding

  1. National Science and Technology Development Agency (NSTDA), Thailand
  2. JSPS Invitation Fellowship Program for Research in Japan
  3. Ministry of Education, Science and Culture of Japan
  4. International Center for Green Biotechnology of Meijo University
  5. Grants-in-Aid for Scientific Research [15K18743] Funding Source: KAKEN

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The cytoplasmic free Ca2+ could play an important role for salt tolerance in rice root (Oryza sativa L.). Here, we compared the expression profiles of two putative developmentally regulated plasma membrane polypeptides (DREPP1 and DREPP2) in rice roots of salt-tolerant cv. Pokkali and salt-sensitive cv. IR29. The messenger RNA (mRNA) for OsDREPP1 could be detected in all parts of root and did not change upon salt stress, whereas the mRNA for OsDREPP2 was detected only in root tips. The transcript level of OsDREPP2 first disappeared upon salt stress, then recovered in Pokkali, but not recovered in IR29. The gene-encoding OsDREPP2 was cloned from cv. Pokkali and expressed in Escherichia coli, and its biochemical properties were studied. It was found that OsDREPP2 is a Ca2+-binding protein and binds also to calmodulin (CaM) as well as microtubules. The mutation of Trp4 and Phe16 in OsDREPP2 to Ala decreased the binding of DREPP2 to Ca2+/CaM complex, indicating the N-terminal basic domain is involved for the binding. The binding of OsDREPP2 to microtubules was inhibited by Ca2+/CaM complex, while the binding of double-mutant OsDREPP2 protein to microtubules was not inhibited by Ca2+/CaM complex. We propose that CaM inhibits the binding of DREPP2 to cortical microtubules, causes the inhibition of microtubule depolymerization, and enhances the cell elongation.

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